A comparison of two models of follow-up care for adult survivors of childhood cancer von Reynolds, K., Spavor, M., Brandelli, Y., Kwok, C., Li, Y., Disciglio, M., Carlson, L. E., Schulte, F., Anderson, R., Grundy, P., Giese-Davis, J.

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Doula care across the maternity care continuum and impact on maternal health: Evaluation of doula programs across three states using propensity score matching von Falconi, April M., Bromfield, Samantha G., Tang, Trúc, Malloy, Demetria, Blanco, Denae, Disciglio, RN Susan, Chi, RN Winnie

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Essential oil characterization of Prunus spinosa L., Salvia officinalis L., Eucalyptus globulus L., Melissa officinalis L. and Mentha x piperita L. by a volatolomic approach von Spadaccino, G., Frabboni, L., Petruzzi, F., Disciglio, G., Mentana, A., Nardiello, D., Quinto, M.

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Classic Galactosemia: Clinical and Computational Characterization of a Novel GALT Missense Variant (p.A303D) and a Literature Review von Forte, Giovanna, Buonadonna, Antonia Lucia, Pantaleo, Antonino, Fasano, Candida, Capodiferro, Donatella, Grossi, Valentina, Sanese, Paola, Cariola, Filomena, De Marco, Katia, Lepore Signorile, Martina, Manghisi, Andrea, Guglielmi, Anna Filomena, Simonetti, Simonetta, Laforgia, Nicola, Disciglio, Vittoria, Simone, Cristiano

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Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus von Jacquemont, Sébastien, Reymond, Alexandre, Walters, Robin G., Kutalik, Zoltán, Valsesia, Armand, Belfiore, Marco, Bouquillon, Sonia, Campion, Dominique, de Vries, Bert B. A., Esko, Tõnu, Hoyer, Juliane, Jarvelin, Marjo-Riitta, Frank Kooy, R., Kurg, Ants, Le Caignec, Cédric, Männik, Katrin, Platt, Orah S., Sanlaville, Damien, Wu, Bai-lin, Yu, Yongguo, Addor, Marie-Claude, Antonarakis, Stylianos E., Arveiler, Benoît, Barth, Magalie, Bergmann, Sven, Bernardini, Laura, Blaumeiser, Bettina, Bonneau, Dominique, Brunner, Han G., Cailley, Dorothée, Chrast, Jacqueline, Coutton, Charles, Cuisset, Jean-Marie, de Freminville, Bénédicte, Demeer, Bénédicte, Descamps, Dominique, Disciglio, Vittoria, Doco-Fenzy, Martine, Dubourg, Christèle, El-Sayed Moustafa, Julia S., Faivre, Laurence, Ferrarini, Alessandra, Fisher, Richard, Flori, Elisabeth, Forer, Lukas, Gaillard, Dominique, Gimelli, Stefania, Gimelli, Giorgio, Grabe, Hans J., Hartikainen, Anna-Liisa, Heron, Délphine, Homuth, Georg, Isidor, Bertrand, Jaillard, Sylvie, Jaros, Zdenek, Jiménez-Murcia, Susana, Joly Helas, Géraldine, Jonveaux, Philippe, Kaksonen, Satu, Kroisel, Peter M., Kronenberg, Florian, Labalme, Audrey, Legallic, Solenn, Lewis, Suzanne, Lucas, Josette, MacDermot, Kay D., Marshall, Christian, McCarthy, Mark I., Meitinger, Thomas, Merla, Giuseppe, Morice-Picard, Fanny, Mucciolo, Mafalda, Nauck, Matthias, Nordgren, Ann, Pasquier, Laurent, Petit, Florence, Plessis, Ghislaine, Paolo Ramelli, Gian, Rauch, Anita, Ravazzolo, Roberto, Roetzer, Katharina M., Rooryck, Caroline, Schurmann, Claudia, Stavropoulos, Dimitri J., Tengström, Carola, Tinahones, Francisco J., Vincent-Delorme, Catherine, Visvikis-Siest, Sophie, Vollenweider, Peter, Völzke, Henry, Vulto-van Silfhout, Anneke T., Waeber, Gérard, Wallgren-Pettersson, Carina, Witwicki, Robert M., Andrieux, Joris, Estivill, Xavier, Gusella, James F., Stefansson, Kari, Beckmann, Jacques S., Froguel, Philippe

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A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders von Zufferey, Flore, Sherr, Elliott H, Beckmann, Noam D, Hanson, Ellen, Maillard, Anne M, Hippolyte, Loyse, Macé, Aurélien, Ferrari, Carina, Kutalik, Zoltán, Andrieux, Joris, Aylward, Elizabeth, Barker, Mandy, Bernier, Raphael, Bouquillon, Sonia, Conus, Philippe, Delobel, Bruno, Faucett, W Andrew, Goin-Kochel, Robin P, Grant, Ellen, Harewood, Louise, Hunter, Jill V, Lebon, Sébastien, Ledbetter, David H, Martin, Christa Lese, Männik, Katrin, Martinet, Danielle, Mukherjee, Pratik, Ramocki, Melissa B, Spence, Sarah J, Steinman, Kyle J, Tjernagel, Jennifer, Spiro, John E, Reymond, Alexandre, Beckmann, Jacques S, Chung, Wendy K, Jacquemont, Sébastien

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Interstitial 22q13 deletions not involving SHANK3 gene: A new contiguous gene syndrome von Disciglio, Vittoria, Rizzo, Caterina Lo, Mencarelli, Maria Antonietta, Mucciolo, Mafalda, Marozza, Annabella, Di Marco, Chiara, Massarelli, Antonio, Canocchi, Valentina, Baldassarri, Margherita, Ndoni, Enea, Frullanti, Elisa, Amabile, Sonia, Anderlid, Britt Marie, Metcalfe, Kay, Le Caignec, Cédric, David, Albert, Fryer, Alan, Boute, Odile, Joris, Andrieux, Greco, Donatella, Pecile, Vanna, Battini, Roberta, Novelli, Antonio, Fichera, Marco, Romano, Corrado, Mari, Francesca, Renieri, Alessandra

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Characterization of a rare variant (c.2635-2A>G) of the MSH2 gene in a family with Lynch syndrome von Cariola, Filomena, Disciglio, Vittoria, Valentini, Anna M., Lotesoriere, Claudio, Fasano, Candida, Forte, Giovanna, Russo, Luciana, Di Carlo, Antonio, Guglielmi, Floranna, Manghisi, Andrea, Lolli, Ivan, Caruso, Maria L., Simone, Cristiano

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Xq28 duplications including MECP2 in five females: Expanding the phenotype to severe mental retardation von Bijlsma, E.K, Collins, A, Papa, F.T, Tejada, M.I, Wheeler, P, Peeters, E.A.J, Gijsbers, A.C.J, van de Kamp, J.M, Kriek, M, Losekoot, M, Broekma, A.J, Crolla, J.A, Pollazzon, M, Mucciolo, M, Katzaki, E, Disciglio, V, Ferreri, M.I, Marozza, A, Mencarelli, M.A, Castagnini, C, Dosa, L, Ariani, F, Mari, F, Canitano, R, Hayek, G, Botella, M.P, Gener, B, Mínguez, M, Renieri, A, Ruivenkamp, C.A.L

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Investigation of modifier genes within copy number variations in Rett syndrome von Artuso, Rosangela, Papa, Filomena T, Grillo, Elisa, Mucciolo, Mafalda, Yasui, Dag H, Dunaway, Keith W, Disciglio, Vittoria, Mencarelli, Maria A, Pollazzon, Marzia, Zappella, Michele, Hayek, Giuseppe, Mari, Francesca, Renieri, Alessandra, LaSalle, Janine M, Ariani, Francesca

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Erratum: Investigation of modifier genes within copy number variations in Rett syndrome von Artuso, Rosangela, Papa, Filomena T, Grillo, Elisa, Mucciolo, Mafalda, Yasui, Dag H, Dunaway, Keith W, Disciglio, Vittoria, Mencarelli, Maria A, Pollazzon, Marzia, Zappella, Michele, Hayek, Giuseppe, Mari, Francesca, Renieri, Alessandra, LaSalle, Janine M, Ariani, Francesca

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Investigation of modifier genes within copy number variations in Rett syndrome von Artuso, Rosangela, Papa, Filomena T, Grillo, Elisa, Mucciolo, Mafalda, Yasui, Dag H, Dunaway, Keith W, Disciglio, Vittoria, Mencarelli, Maria A, Pollazzon, Marzia, Zappella, Michele, Hayek, Giuseppe, Mari, Francesca, Renieri, Alessandra, LaSalle, Janine M, Ariani, Francesca

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